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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2309205Generated: October 25, 2026

Methyl p-toluenesulfonate → Methyl 2-amino-6-nitrobenzoate

https://huagongshe.com/reaction/2309205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl p-toluenesulfonateHCID 6645—
ReactantTriethylamineHCID 8471—
Reactant2-Amino-6-nitro-benzoic acidHCID 95795—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-amino-6-nitrobenzoateHCID 596477—

Reaction Steps

A mixture of 2-amino-6-nitrobenzoic acid (11.9 g, 65.3 mmol), methyl p-toluenesulfonate (15.1 g, 81.1 mmol) and triethylamine (6.60 g, 65.3 mmol) in DMF (170 ml) was stirred under N2 at 60° for 18 hours. After removing DMF at 60° and 0.2 mm pressure, the residue was dissolved in ETOAc and washed with a saturated solution of NaHCO3 followed by a saturated aqueous solution of NaCl. The EtOAc extract was dried (Na2SO4) , filtered and concentrated under reduced pressure. Flash chromatography over silica gel and elution with 50% toluene-50% CHCl3 gave methyl 2-amino-6-nitrobenzoate benzote (7.6 g, 59.4%), m.p. 105°-107°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04694020
Source datasetuspto-grants-1987_09
ORD IDord-c955f523054e43b38201f124c7576520
Source noteuspto-grants-1987_09